Reaction Details Report a problem with these data
Target
Glutamate racemase
Ligand
BDBM50262011
Substrate
n/a
Meas. Tech.
ChEMBL_514356 (CHEMBL967970)
IC50
27±n/a nM
Citation
 Basarab, GS; Hill, PJ; Rastagar, A; Webborn, PJ Design of Helicobacter pylori glutamate racemase inhibitors as selective antibacterial agents: a novel pro-drug approach to increase exposure. Bioorg Med Chem Lett 18:4716-22 (2008) [PubMed]  Article 
Target
Name:
Glutamate racemase
Synonyms:
MURI_HELPY | glr | murI
Type:
PROTEIN
Mol. Mass.:
28413.39
Organism:
Helicobacter pylori
Description:
ChEMBL_475324
Residue:
255
Sequence:
MKIGVFDSGVGGFSVLKSLLKAQLFDEIIYYGDSARVPYGTKDPTTIKQFGLEALDFFKPHQIKLLIVACNTASALALEEMQKHSKIPVVGVIEPSILAIKRQVKDKNAPILVLGTKATIQSNAYDNALKQQGYLNVSHLATSLFVPLIEESILEGELLETCMRYYFTPLEILPEVVILGCTHFPLIAQKIEGYFMEHFALSTPPLLIHSGDAIVEYLQQNYALKKNACAFPKVEFHASGDVVWLEKQAKEWLKL
  
Inhibitor
Name:
BDBM50262011
Synonyms:
5-(2-((5-chloro-1H-indol-3-yl)methyl)-7-(cyclopropylmethyl)-5-methyl-4,6-dioxo-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-d]pyrimidin-3-yl)-N,1-dimethyl-1H-pyrrole-3-sulfonamide | CHEMBL467999
Type:
Small organic molecule
Emp. Form.:
C25H26ClN7O4S
Mol. Mass.:
556.036
SMILES:
CNS(=O)(=O)c1cc(-c2n(Cc3c[nH]c4ccc(Cl)cc34)nc3n(CC4CC4)c(=O)n(C)c(=O)c23)n(C)c1 |(26.84,5.41,;25.5,6.17,;24.18,5.39,;23.33,6.68,;25.03,4.1,;22.94,4.48,;22.94,2.94,;21.48,2.46,;21.01,1,;21.92,-.25,;23.46,-.25,;24.23,-1.59,;23.61,-2.99,;24.75,-4.02,;26.08,-3.25,;27.54,-3.72,;28.68,-2.7,;28.36,-1.19,;29.5,-.16,;26.9,-.72,;25.76,-1.74,;21.01,-1.51,;19.53,-1.03,;18.19,-1.8,;18.19,-3.34,;16.85,-4.1,;15.31,-4.11,;16.08,-5.44,;16.85,-1.03,;15.52,-1.8,;16.85,.52,;15.52,1.29,;18.19,1.3,;18.19,2.84,;19.53,.52,;20.58,3.71,;19.04,3.71,;21.48,4.95,)|
Structure:
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